NIH-funded research P01 program project

New strategies to boost regulatory T cells and pause immunosuppressants after kidney transplant

Official title: Innovative strategies to enhance Treg function and promote IS drug-free kidney transplant survival

Funded at University of Pittsburgh at Pittsburgh · NIH-11365827 · Data updated 2026-11-12

This grant explores using engineered immune cells to help kidney transplant patients keep a healthy graft without lifelong immunosuppressive drugs.

More Transplant research and trials

Quick facts

Grant typeP01 program project
Study typeNIH-funded research
Funding institutionUniversity of Pittsburgh at Pittsburgh
NIH-funded
Lab location1 site (Pittsburgh, United States)
Project startJuly 3, 2025
Project endMay 31, 2030
Funding year2026
Award (this year)$780,506
NIH project number5P01AI181829-02
Project IDNIH-11365827 on NIH RePORTER

Who could benefit from this research

Could help

Adults who have или may undergo kidney transplantation and are candidates for tolerogenic cell therapies involving regulatory T cells or CARTreg approaches.

Less likely to help

Individuals not eligible for cellular therapy or with contraindications to cell-based tolerance strategies may not benefit.

What this research studies

Researchers aim to prolong immunosuppression-free graft survival by restraining memory T cells that resist standard therapy and by boosting donor-specific regulatory T cells. The project includes ex vivo expansion and genetic shaping of regulatory T cells (including CARTreg) to target donor antigens and improve their function after transfer into patients. The work examines how to balance inflammation, antigen-presenting cells, and cytokines to support durable tolerance while minimizing side effects. The study translates promising findings from animal models toward human kidney transplant patients, with a focus on achieving long-term graft acceptance without persistent immunosuppression.

Why it matters

Potential benefit: If successful, patients could maintain kidney graft function without lifelong immunosuppressive medications and their associated harms.

How similar studies have gone: Early preclinical data and rodent transplant studies support the potential of regulatory T cell–based strategies to promote tolerance, with ongoing translation to human-focused work.

Where this research is happening

  • University of Pittsburgh at Pittsburgh
    Pittsburgh, United States
    Active

Researchers

  • Principal investigator: Ezzelarab, Mohamed B — University of Pittsburgh at Pittsburgh
  • Study coordinator: Ezzelarab, Mohamed B

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.